Renal distribution of collagen type IV α chains in autosomal-dominant Alport syndrome

被引：0
作者：
Ichiro Naito
Shinsuke Nomura
Shinichiro Kawai
Satoko Inoue
J. Ashley Jefferson
Claire M. Hill
Takashi Harada
Yoshikazu Sado
Gengo Osawa
机构：
[1] Shigei Medical Research Institute,Division of Immunology
[2] Kawasaki Medical School,Division of Nephrology, Department of Medicine
[3] Shigei Hospital,Division of Internal Medicine
[4] Belfast City Hospital,Department of Nephrology
[5] Queen's University of Belfast,Department of Medical Genetics and Pathology
[6] Nagasaki University Hospital,Renal Care Unit
[7] Shigei Medical Research Institute,Division of Ultrastructural Biology
来源：
Clinical and Experimental Nephrology | 1998年 / 2卷 / 1期
关键词：
Alport syndrome; type IV collagen; hereditary nephritis; immunohistochemistry; monoclonal antibody; antigen retrieval;
D O I：
10.1007/BF02480625
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：58 / 63
页数：5
相关论文
共 50 条
  • [21] Familial hematuria due to type IV collagen mutations: Alport syndrome and thin basement membrane nephropathy
    Kashtan, CE
    CURRENT OPINION IN PEDIATRICS, 2004, 16 (02) : 177 - 181
  • [22] Type IV collagen α chains in colon cancer
    Hiki, Y
    Iyama, K
    Egami, H
    Ogawa, M
    BIOLOGICAL RESPONSE TO PLANNED AND UNPLANNED INJURIES: CELLULAR, MOLECULAR AND GENETIC ASPECTS, 2003, 1255 : 321 - 324
  • [23] Fibromuscular dysplasia with moyamoya phenomenon in a patient with Alport's syndrome.: A type IV collagen disorder
    Escamilla, F
    Espigares, A
    Hervás, R
    Fernández, MD
    Vela, R
    García, T
    REVISTA DE NEUROLOGIA, 2000, 30 (08) : 736 - 740
  • [24] Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome
    Koyama, Yuimi
    Suico, Mary Ann
    Owaki, Aimi
    Sato, Ryoichi
    Kuwazuru, Jun
    Kaseda, Shota
    Sannomiya, Yuya
    Horizono, Jun
    Omachi, Kohei
    Horinouchi, Tomoko
    Yamamura, Tomohiko
    Tsuhako, Haruki
    Nozu, Kandai
    Shuto, Tsuyoshi
    Kai, Hirofumi
    CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2024, 28 (09) : 874 - 881
  • [25] Immunolocalization and distribution patterns of type IV collagen alpha chains in oral mucosal melanoma
    Nagatsuka, H
    Rivera, RS
    Gunduz, M
    Lee, YJ
    Tamamura, R
    Gunduz, E
    Naito, I
    Sado, Y
    Nagai, N
    VIRCHOWS ARCHIV, 2005, 447 (04) : 710 - 716
  • [26] Immunolocalization and distribution patterns of type IV collagen alpha chains in oral mucosal melanoma
    Hitoshi Nagatsuka
    Rosario Santos Rivera
    Mehmet Gunduz
    You-Jin Lee
    Ryo Tamamura
    Esra Gunduz
    Ichiro Naito
    Yoshikazu Sado
    Noriyuki Nagai
    Virchows Archiv, 2005, 447 : 710 - 716
  • [27] Collagen COL4A3 knockout: A mouse model for autosomal Alport syndrome
    Cosgrove, D
    Meehan, DT
    Grunkemeyer, JA
    Kornak, JM
    Sayers, R
    Hunter, WJ
    Samuelson, GC
    GENES & DEVELOPMENT, 1996, 10 (23) : 2981 - 2992
  • [28] Case Report: Identification of a Novel Heterozygous Missense Mutation in COL4A3 Gene Causing Variable Phenotypes in an Autosomal-Dominant Alport Syndrome Family
    Hu, Yanglin
    Li, Wei
    Tian, Lulu
    Fu, Shuai
    Min, Yonglong
    Liu, Jia
    Xiong, Fei
    FRONTIERS IN GENETICS, 2022, 13
  • [29] Glomerular basement membrane type IV collagen antigens in Goodpasture's and Alport's syndromes
    Yoshikazu Sado
    Ichiro Naito
    Yoshifumi Ninomiya
    Clinical and Experimental Nephrology, 1998, 2 (4) : 282 - 288
  • [30] Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group
    Kashtan, Clifford E.
    Ding, Jie
    Garosi, Guido
    Heidet, Laurence
    Massella, Laura
    Nakanishi, Koichi
    Nozu, Kandai
    Renieri, Alessandra
    Rheault, Michelle
    Wang, Fang
    Gross, Oliver
    KIDNEY INTERNATIONAL, 2018, 93 (05) : 1045 - 1051
12345